Characterization of early endosome antigen 1 in neural tissues

被引:6
作者
Selak, S
Braun, JE
Fritzler, MJ [1 ]
机构
[1] Univ Calgary, Fac Med, Dept Biochem & Mol Biol, Calgary, AB, Canada
[2] Inst Cajal, Dept Neural Plastic, Madrid, Spain
[3] Univ Calgary, Fac Med, Dept Physiol & Biophys, Calgary, AB, Canada
基金
加拿大健康研究院;
关键词
autoantibodies; endosomes; autoimmunity; neurological disease; synaptic vesicles;
D O I
10.1016/j.bbrc.2004.09.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The finding that patients and mice bearing autoantibodies directed against early endosome antigen 1 (EEA1) develop neurological signs and deficits prompted an investigation of EEA1 distribution, localization, and interaction with synaptic proteins found in neural tissues. We detected EEA1 in a variety of neural tissues and in cells of neural origin where it co-localized with SNAP-25. The interaction between EEA1 and SNAP-25 was dependent on the leucine zipper and a newly identified methyl-accepting domain of EEA1. The C-terminal zinc-binding FYVE finger motif (EEA1(1271-1411)) of EEA1 also interacted with native SNAP-25 but only in the presence of 100 muM Ca2+. In contrast, EEA1 did not bind to cysteine string protein or synapsin in these binding assays. These results suggest that EEA1 is involved in neuronal synaptic vesicle function and axonal transport and growth. EEA1 may undergo calcium-dependent conformational changes that are required for binding to SNAP-25. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1334 / 1342
页数:9
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